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PUBMED FOR HANDHELDS

Journal Abstract Search


146 related items for PubMed ID: 22197475

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  • 3. A novel pathway for arsenic elimination: human multidrug resistance protein 4 (MRP4/ABCC4) mediates cellular export of dimethylarsinic acid (DMAV) and the diglutathione conjugate of monomethylarsonous acid (MMAIII).
    Banerjee M, Carew MW, Roggenbeck BA, Whitlock BD, Naranmandura H, Le XC, Leslie EM.
    Mol Pharmacol; 2014 Aug; 86(2):168-79. PubMed ID: 24870404
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  • 8. Stability of arsenic metabolites, arsenic triglutathione [As(GS)3] and methylarsenic diglutathione [CH3As(GS)2], in rat bile.
    Kobayashi Y, Cui X, Hirano S.
    Toxicology; 2005 Jul 01; 211(1-2):115-23. PubMed ID: 15863254
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  • 9. Biliary excretion of arsenic by human HepaRG cells is stimulated by selenide and mediated by the multidrug resistance protein 2 (MRP2/ABCC2).
    Zhou JR, Kaur G, Ma Y, Arutyunov D, Lu X, Le XC, Leslie EM.
    Biochem Pharmacol; 2021 Nov 01; 193():114799. PubMed ID: 34678219
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  • 10. Arsenic Triglutathione [As(GS)3] Transport by Multidrug Resistance Protein 1 (MRP1/ABCC1) Is Selectively Modified by Phosphorylation of Tyr920/Ser921 and Glycosylation of Asn19/Asn23.
    Shukalek CB, Swanlund DP, Rousseau RK, Weigl KE, Marensi V, Cole SP, Leslie EM.
    Mol Pharmacol; 2016 Aug 01; 90(2):127-39. PubMed ID: 27297967
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  • 11. The accumulation and toxicity of methylated arsenicals in endothelial cells: important roles of thiol compounds.
    Hirano S, Kobayashi Y, Cui X, Kanno S, Hayakawa T, Shraim A.
    Toxicol Appl Pharmacol; 2004 Aug 01; 198(3):458-67. PubMed ID: 15276427
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  • 13. Modulation of human multidrug resistance protein (MRP) 1 (ABCC1) and MRP2 (ABCC2) transport activities by endogenous and exogenous glutathione-conjugated catechol metabolites.
    Slot AJ, Wise DD, Deeley RG, Monks TJ, Cole SP.
    Drug Metab Dispos; 2008 Mar 01; 36(3):552-60. PubMed ID: 18079363
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  • 14. Polymorphic variants of MRP4/ABCC4 differentially modulate the transport of methylated arsenic metabolites and physiological organic anions.
    Banerjee M, Marensi V, Conseil G, Le XC, Cole SP, Leslie EM.
    Biochem Pharmacol; 2016 Nov 15; 120():72-82. PubMed ID: 27659809
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  • 15. A new metabolic pathway of arsenite: arsenic-glutathione complexes are substrates for human arsenic methyltransferase Cyt19.
    Hayakawa T, Kobayashi Y, Cui X, Hirano S.
    Arch Toxicol; 2005 Apr 15; 79(4):183-91. PubMed ID: 15526190
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  • 16. Structural determinants of substrate specificity differences between human multidrug resistance protein (MRP) 1 (ABCC1) and MRP3 (ABCC3).
    Grant CE, Gao M, DeGorter MK, Cole SP, Deeley RG.
    Drug Metab Dispos; 2008 Dec 15; 36(12):2571-81. PubMed ID: 18775981
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  • 17. Glutathione synthetase promotes the reduction of arsenate via arsenolysis of glutathione.
    Németi B, Anderson ME, Gregus Z.
    Biochimie; 2012 Jun 15; 94(6):1327-33. PubMed ID: 22426003
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  • 18. Human red blood cell uptake and sequestration of arsenite and selenite: Evidence of seleno-bis(S-glutathionyl) arsinium ion formation in human cells.
    Kaur G, Javed W, Ponomarenko O, Shekh K, Swanlund DP, Zhou JR, Summers KL, Casini A, Wenzel MN, Casey JR, Cordat E, Pickering IJ, George GN, Leslie EM.
    Biochem Pharmacol; 2020 Oct 15; 180():114141. PubMed ID: 32652143
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  • 19. Identification and Functional Characterization of a GSH Conjugate Efflux Pathway in the Rat Lens.
    Umapathy A, Li B, Donaldson PJ, Lim JC.
    Invest Ophthalmol Vis Sci; 2015 Aug 15; 56(9):5256-68. PubMed ID: 26244301
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  • 20. Differential Selectivity of Human and Mouse ABCC4/Abcc4 for Arsenic Metabolites.
    Whitlock BD, Ma Y, Conseil G, O'Brien AR, Banerjee M, Swanlund DP, Lin ZP, Wang Y, Le XC, Schuetz JD, Cole SPC, Leslie EM.
    Drug Metab Dispos; 2024 Nov 15; 52(12):1417-1428. PubMed ID: 39313329
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